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Data · dataset · 2026

Atg8-associated regulatory module coordinates autophagy and ubiquitin-mediated proteostasis in Peronophythora litchii

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Autophagy is a conserved eukaryotic degradation pathway that plays essential roles in growth, development, and pathogenicity in plant-pathogenic oomycetes.

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In this study, we identified two PlAtg8-interacting proteins in Peronophythora litchii: the peroxisomal membrane protein PlPex13 and the methyltransferase PlDph5. These proteins form an Atg8-associated interaction module through pairwise interactions and subcellular colocalization.

Functional analyses revealed that PlDph5 is a positive regulator of macroautophagy, as its deletion significantly impairs autophagosome formation and autophagic flux. In contrast, PlPex13 is dispensable for bulk autophagy but is involved in pexophagy-associated turnover and localizes to peroxisomes. Both PlPex13 and PlDph5 are required for normal vegetative growth, asexual reproduction, and pathogenicity of P. litchii.

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In addition, PlPex13 undergoes ubiquitination and proteasome-associated turnover, and disruption of PlDph5 alters global ubiquitinated protein homeostasis. Collectively, our findings identify a PlAtg8 associated regulatory module comprising PlPex13 and PlDph5 that integrates autophagy and ubiquitin-mediated protein turnover to coordinate cellular homeostasis, development, and pathogenicity in P. litchii.

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Evolutionary biology 69%
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